TY - JOUR
T1 - A novel three-dimensional culture system for isolation and clonal propagation of neural stem cells using a thermo-reversible gelation polymer
AU - Yang, Xin Zhi
AU - Kataoka, Ken
AU - Medina, Reinhold
AU - Yamamoto, Ken Ichi
AU - Than, Swe Swe
AU - Miyazaki, Masahiro
AU - Huh, Nam Ho
PY - 2009/12/1
Y1 - 2009/12/1
N2 - In the present study, we examined the possible utility of a three-dimensional culture system using a thermo-reversible gelation polymer to isolate and expand neural stem cells (NSCs). The polymer is a synthetic biologically inert polymer and gelates at temperatures higher than the gel-sol transition point (∼20°C). When fetal mouse brain cells were inoculated into the gel, spherical colonies were formed (∼1% in primary culture and ∼9% in passage cultures). The spheroid-forming cells were positive for expression of the NSC markers nestin and Musashi. Under conditions facilitating spontaneous neural differentiation, the spheroid-forming cells expressed genes characteristic to astrocytes, oligodendrocytes, and neurons. The cells could be successively propagated at least to 80 poly-D-lysines over a period of 20 weeks in the gel culture with a growth rate higher than that observed in suspension culture. The spheroids formed by fetal mouse brain cells in the gel were shown to be of clonal origin. These results indicate that the spheroid culture system is a convenient and powerful tool for isolation and clonal expansion of NSCs in vitro.
AB - In the present study, we examined the possible utility of a three-dimensional culture system using a thermo-reversible gelation polymer to isolate and expand neural stem cells (NSCs). The polymer is a synthetic biologically inert polymer and gelates at temperatures higher than the gel-sol transition point (∼20°C). When fetal mouse brain cells were inoculated into the gel, spherical colonies were formed (∼1% in primary culture and ∼9% in passage cultures). The spheroid-forming cells were positive for expression of the NSC markers nestin and Musashi. Under conditions facilitating spontaneous neural differentiation, the spheroid-forming cells expressed genes characteristic to astrocytes, oligodendrocytes, and neurons. The cells could be successively propagated at least to 80 poly-D-lysines over a period of 20 weeks in the gel culture with a growth rate higher than that observed in suspension culture. The spheroids formed by fetal mouse brain cells in the gel were shown to be of clonal origin. These results indicate that the spheroid culture system is a convenient and powerful tool for isolation and clonal expansion of NSCs in vitro.
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U2 - 10.1089/ten.tec.2008.0516
DO - 10.1089/ten.tec.2008.0516
M3 - Article
C2 - 19231918
AN - SCOPUS:72249083521
SN - 1937-3384
VL - 15
SP - 615
EP - 623
JO - Tissue Engineering - Part C: Methods
JF - Tissue Engineering - Part C: Methods
IS - 4
ER -